Canonical Allele Identifier: PA106388
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102905
ClinVar RCV Id: RCV000089169 RCV000758098
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro314Ser
CA229865
NM_000277.3:c.940C>T